What are the responsibilities and job description for the Immediate Job Opportunity for Validation Engineer I position at The Fountain Group?
The Fountain Group is currently seeking an Validation Engineer I for a prominent client of ours. This position is located in Vacaville, CA. Details for the position are as follows:
Title: Validation Engineer I
Location: Vacaville, CA 95688, USA
Duration: 6 months (Possible extension/conversion based on performance and budget)
Hourly Rate on W2: $30 - $44/hr.
Job Description:
With direct supervision, candidate is responsible for support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and company corporate principals, quality policies, standards, and core values. Maintains company’s right to operate, supply to patients, and cost effectiveness by actively participating in continuous improvement projects.
Technical Duties:
Education:
Standard office environment
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Title: Validation Engineer I
Location: Vacaville, CA 95688, USA
Duration: 6 months (Possible extension/conversion based on performance and budget)
Hourly Rate on W2: $30 - $44/hr.
Job Description:
With direct supervision, candidate is responsible for support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and company corporate principals, quality policies, standards, and core values. Maintains company’s right to operate, supply to patients, and cost effectiveness by actively participating in continuous improvement projects.
Technical Duties:
- Perform qualification of laboratory equipment in accordance with EQ policies, plans and procedures.
- Coordinate with laboratory personnel to define qualification requirements.
- Author, review and execute equipment qualification protocols.
- Coordinate equipment qualification activities with vendors and other support groups.
- Identify business, quality, and compliance gaps.
- Sign documents for activities as authorized and described by policies, procedures and job descriptions.
- Perform any other tasks as requested by Senior Management to support QC laboratory operations.
Education:
- BS/BA degree (preferably in relevant scientific discipline)
- Experience (may vary depending on site size/scope)
- Experience in the pharmaceutical, biopharmaceutical industry or an equivalent combination of education and experience.
- Knowledge of cGMP or equivalent regulations.
- Minimum of two years’ experience in Validation or equipment qualification is desired.
- Ability to make sound decisions about scheduling and managing of priorities.
- Flexibility in problem solving, providing direction and work hours to meet business objectives.
- Possesses strong verbal and written communication skills and the ability to influence at all levels
- Capable of building trustful and effective relationships
- Able to think strategically and translate strategies into actionable plans
- Takes responsibility, drives results, and achieves expected outcomes
Standard office environment
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy
#ZIP
Salary : $30 - $44